N/A
Completed N=655
Brief Video Interventions for Depression
Source: ClinicalTrials.gov NCT04643964 ↗Enrolled (actual)
655
Serious AEs
—
Results posted
May 2024
Primary outcomePrimary: Change in the Quick Inventory of Depressive Symptoms-Self Report (QIDS-SR) — 13.67; 14.09; 14.29; 13.79 units on a scale — p=.54
Summary
In this study, we test brief video interventions for those with elevated depressive symptoms. We randomize participants to one of three conditions. (1) An entrée condition involving in-depth coverage a set of cognitive behavioral therapy (CBT) skills. (2) A sampler condition which introduces three sets of CBT skills. (3) A control condition involving no skills. Among those in the entrée condition, participants are further randomized to one of three CBT skills. We plan on two sets of primary comparisons. First, we will compare the effects of each form of video intervention (i.e., entrée and sampler) to the control condition. Second, we will compare the entrée and sampler conditions. We will recruit participants from Amazon's Mechanical Turk program (MTurk). In the intervention conditions, participants will be asked to watch several videos and practice skills using worksheets. They will also be asked to practice skills introduced in the videos in the week following the intervention. In the control condition, participants will not watch videos. One week after the intervention, all participants will respond to a follow-up assessment.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Change in the Quick Inventory of Depressive Symptoms-Self Report (QIDS-SR) |
13.67; 14.09; 14.29; 13.79; 14.03; 13.00 | .54 |
| SECONDARY Change in the Ways of Responding Questionnaire (WOR) |
3.58; 3.70; 3.71; 3.70; 3.7; 3.88 | .92 |
| SECONDARY Change in the Styles of Emotion Response Questionnaire (SERQ) |
33.45; 32.85; 33.31; 32.69; 32.57; 33.41 | .37 |
| SECONDARY Change in the University of California, Los Angeles (UCLA) Loneliness Scale, Version 3 |
53.87; 55.80; 54.70; 53.97; 54.66; 52.59 | .87 |
Eligibility Criteria
Inclusion Criteria
- Score above 10 on the Patient Health Questionnaire-9
- Are 18 years of age or older
Data sourced from ClinicalTrials.gov (NCT04643964). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.